LENS 4K Camera Head 72205058

GUDID 00885556720790

LENS 4K A/C CAMERA HEAD

Smith & Nephew, Inc.

Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit

• Primary Device ID: 00885556720790
• NIH Device Record Key: 412c34c6-ed17-48ea-b7c9-4d7e07a203d3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LENS 4K Camera Head
• Version Model Number: 72205058
• Catalog Number: 72205058
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556720790 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191177

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

[00885556720790]

Liquid Chemical;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-09-26
• Device Publish Date: 2019-09-18

Devices Manufactured by Smith & Nephew, Inc.

• 00885556747353 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 LEFT
• 00885556747360 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 LEFT
• 00885556747377 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 LEFT
• 00885556747384 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 5 LEFT
• 00885556747407 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 RIGHT
• 00885556747414 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 RIGHT
• 00885556747421 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 RIGHT
• 00885556747438 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 4 RIGHT